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Artigo de periodico
WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease (2023)
Ferrari, M. T. M; Watanabe, A; Silva, T. E. Da; Gomes, N. L; Batista, R. L; Nishi, M. Y; Paula, L. C. P. De; COSTA, E. C; Onuchic, Luiz Fernando ; Mendonca, Berenice Bilharinho de
Source: Sexual development. Unidade: FM
Subjects: NEOPLASIAS RENAIS, GENES SUPRESSORES DE TUMOR
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FERRARI, M. T. M et al. WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease. Sexual development, v. 16, n. 1, p. 46-54, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58605. Acesso em: 01 nov. 2024.
APA
Ferrari, M. T. M., Watanabe, A., Silva, T. E. D., Gomes, N. L., Batista, R. L., Nishi, M. Y., et al. (2023). WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease. Sexual development, 16( 1), 46-54. doi:10.1159/000517373
NLM
Ferrari MTM, Watanabe A, Silva TED, Gomes NL, Batista RL, Nishi MY, Paula LCPD, COSTA EC, Onuchic LF, Mendonca BB de. WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease [Internet]. Sexual development. 2023 ; 16( 1): 46-54.[citado 2024 nov. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58605
Vancouver
Ferrari MTM, Watanabe A, Silva TED, Gomes NL, Batista RL, Nishi MY, Paula LCPD, COSTA EC, Onuchic LF, Mendonca BB de. WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease [Internet]. Sexual development. 2023 ; 16( 1): 46-54.[citado 2024 nov. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58605
Artigo de periodico
Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications (2023)
Silva, Fernanda Jardim da; Azevedo Junior, Juscelino Carvalho de; Ralph, Ana Carolina Lima ; Pinheiro, João de Jesus Viana ; Calcagno, Danielle Queiroz ; Freitas, Vanessa Morais
Source: Frontiers in Oncology. Unidades: ICB, FM
Subjects: BIOLOGIA CELULAR, NEOPLASIAS DE CABEÇA E PESCOÇO, ADENOIDES, GLÂNDULAS SALIVARES, METÁSTASE NEOPLÁSICA, CROMATINA, CÉLULAS CULTIVADAS DE TUMOR, GENES SUPRESSORES DE TUMOR, MUTAÇÃO GENÉTICA
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SILVA, Fernanda Jardim da et al. Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications. Frontiers in Oncology, v. 13, p. 1-14, 2023Tradução . . Disponível em: https://doi.org/10.3389/fonc.2023.1191218. Acesso em: 01 nov. 2024.
APA
Silva, F. J. da, Azevedo Junior, J. C. de, Ralph, A. C. L., Pinheiro, J. de J. V., Calcagno, D. Q., & Freitas, V. M. (2023). Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications. Frontiers in Oncology, 13, 1-14. doi:10.3389/fonc.2023.1191218
NLM
Silva FJ da, Azevedo Junior JC de, Ralph ACL, Pinheiro J de JV, Calcagno DQ, Freitas VM. Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications [Internet]. Frontiers in Oncology. 2023 ; 13 1-14.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3389/fonc.2023.1191218
Vancouver
Silva FJ da, Azevedo Junior JC de, Ralph ACL, Pinheiro J de JV, Calcagno DQ, Freitas VM. Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications [Internet]. Frontiers in Oncology. 2023 ; 13 1-14.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3389/fonc.2023.1191218
Artigo de periodico
Liquid biopsy can detect BRCA2 gene variants in female dogs with mammary neoplasia (2022)
Oliveira, Jéssica Rodrigues; Colombo, Jucimara; Gonçalves, Francine Moraes; Carvalho, Lucas Amoroso Lopes; Costa, Douglas Santos; Henrique, Tiago; Novais, Adriana Alonso; Moschetta‐Pinheiro, Marina Gobbe; Chuffa, Luiz Gustavo de Almeida; Coutinho, Luiz Lehmann ; Santana, Áureo Evangelista; Zuccari, Debora Aparecida Pires de Campos
Source: Veterinary and Comparative Oncology. Unidade: ESALQ
Subjects: BIÓPSIA, CADELAS, CARCINOGÊNESE ANIMAL, GENES SUPRESSORES DE TUMOR, NEOPLASIAS MAMÁRIAS
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OLIVEIRA, Jéssica Rodrigues et al. Liquid biopsy can detect BRCA2 gene variants in female dogs with mammary neoplasia. Veterinary and Comparative Oncology, v. 20, p. 164–171, 2022Tradução . . Disponível em: https://doi.org/10.1111/vco.12758. Acesso em: 01 nov. 2024.
APA
Oliveira, J. R., Colombo, J., Gonçalves, F. M., Carvalho, L. A. L., Costa, D. S., Henrique, T., et al. (2022). Liquid biopsy can detect BRCA2 gene variants in female dogs with mammary neoplasia. Veterinary and Comparative Oncology, 20, 164–171. doi:10.1111/vco.12758
NLM
Oliveira JR, Colombo J, Gonçalves FM, Carvalho LAL, Costa DS, Henrique T, Novais AA, Moschetta‐Pinheiro MG, Chuffa LG de A, Coutinho LL, Santana ÁE, Zuccari DAP de C. Liquid biopsy can detect BRCA2 gene variants in female dogs with mammary neoplasia [Internet]. Veterinary and Comparative Oncology. 2022 ; 20 164–171.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1111/vco.12758
Vancouver
Oliveira JR, Colombo J, Gonçalves FM, Carvalho LAL, Costa DS, Henrique T, Novais AA, Moschetta‐Pinheiro MG, Chuffa LG de A, Coutinho LL, Santana ÁE, Zuccari DAP de C. Liquid biopsy can detect BRCA2 gene variants in female dogs with mammary neoplasia [Internet]. Veterinary and Comparative Oncology. 2022 ; 20 164–171.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1111/vco.12758
Artigo de periodico
Epithelial–mesenchymal transition signaling and prostate cancer stem cells: emerging biomarkers and opportunities for precision therapeutics (2021)
Souza, Luiz Paulo Chaves de; Melo, Camila Morais ; Saggioro, Fabiano Pinto ; Reis, Rodolfo Borges dos ; Squire, Jeremy Andrew
Source: Genes. Unidades: SVOI, FMRP
Subjects: NEOPLASIAS PROSTÁTICAS, IMUNOTERAPIA, ONCOGENES, GENES SUPRESSORES DE TUMOR, MUTAÇÃO GENÉTICA, BIOMARCADORES
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SOUZA, Luiz Paulo Chaves de et al. Epithelial–mesenchymal transition signaling and prostate cancer stem cells: emerging biomarkers and opportunities for precision therapeutics. Genes, v. 12, n. 12, p. 1-18, 2021Tradução . . Disponível em: https://doi.org/10.3390/genes12121900. Acesso em: 01 nov. 2024.
APA
Souza, L. P. C. de, Melo, C. M., Saggioro, F. P., Reis, R. B. dos, & Squire, J. A. (2021). Epithelial–mesenchymal transition signaling and prostate cancer stem cells: emerging biomarkers and opportunities for precision therapeutics. Genes, 12( 12), 1-18. doi:10.3390/genes12121900
NLM
Souza LPC de, Melo CM, Saggioro FP, Reis RB dos, Squire JA. Epithelial–mesenchymal transition signaling and prostate cancer stem cells: emerging biomarkers and opportunities for precision therapeutics [Internet]. Genes. 2021 ; 12( 12): 1-18.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/genes12121900
Vancouver
Souza LPC de, Melo CM, Saggioro FP, Reis RB dos, Squire JA. Epithelial–mesenchymal transition signaling and prostate cancer stem cells: emerging biomarkers and opportunities for precision therapeutics [Internet]. Genes. 2021 ; 12( 12): 1-18.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/genes12121900
Trabalho de evento-resumo
TCGA analysis identifies distinct genomic features of oncogenic progression and outcome associated with hemizygous PTEN loss tumors (2021)
Melo, Camila Morais ; Vidotto, Thiago; Dutra, William Lautert; Souza, Luiz Paulo Chaves de; Reis, Rodolfo Borges dos; Squire, Jeremy Andrew
Source: Resumos. Conference titles: Congresso Brasileiro de Genética = Brazilian Congress of Genetics. Unidade: FMRP
Subjects: GENES SUPRESSORES DE TUMOR, MUTAÇÃO GENÉTICA, CARCINOGÊNESE
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MELO, Camila Morais et al. TCGA analysis identifies distinct genomic features of oncogenic progression and outcome associated with hemizygous PTEN loss tumors. 2021, Anais.. [Ribeirão Preto]: Sociedade Brasileira de Genética - SBG, 2021. Disponível em: https://www.sbg.org.br/anais. Acesso em: 01 nov. 2024.
APA
Melo, C. M., Vidotto, T., Dutra, W. L., Souza, L. P. C. de, Reis, R. B. dos, & Squire, J. A. (2021). TCGA analysis identifies distinct genomic features of oncogenic progression and outcome associated with hemizygous PTEN loss tumors. In Resumos. [Ribeirão Preto]: Sociedade Brasileira de Genética - SBG. Recuperado de https://www.sbg.org.br/anais
NLM
Melo CM, Vidotto T, Dutra WL, Souza LPC de, Reis RB dos, Squire JA. TCGA analysis identifies distinct genomic features of oncogenic progression and outcome associated with hemizygous PTEN loss tumors [Internet]. Resumos. 2021 ;[citado 2024 nov. 01 ] Available from: https://www.sbg.org.br/anais
Vancouver
Melo CM, Vidotto T, Dutra WL, Souza LPC de, Reis RB dos, Squire JA. TCGA analysis identifies distinct genomic features of oncogenic progression and outcome associated with hemizygous PTEN loss tumors [Internet]. Resumos. 2021 ;[citado 2024 nov. 01 ] Available from: https://www.sbg.org.br/anais
Artigo de periodico
Targeting the highly expressed microRNA miR-146b with CRISPR/Cas9n gene editing system in thyroid cancer (2021)
Inez, Daniel Casartelli de Santa ; Fuziwara, Cesar Seigi ; Saito, Kelly Cristina ; Kimura, Edna Teruko
Source: International Journal of Molecular Sciences. Unidade: ICB
Subjects: BIOLOGIA CELULAR, NEOPLASIAS DA TIREOIDE, MICRORNAS, GENES SUPRESSORES DE TUMOR, CÉLULAS CULTIVADAS DE TUMOR, CAMUNDONGOS, SEQUENCIAMENTO GENÉTICO, EXPRESSÃO GÊNICA
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INEZ, Daniel Casartelli de Santa et al. Targeting the highly expressed microRNA miR-146b with CRISPR/Cas9n gene editing system in thyroid cancer. International Journal of Molecular Sciences, v. 22, n. 15, p. 1-14, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms22157992. Acesso em: 01 nov. 2024.
APA
Inez, D. C. de S., Fuziwara, C. S., Saito, K. C., & Kimura, E. T. (2021). Targeting the highly expressed microRNA miR-146b with CRISPR/Cas9n gene editing system in thyroid cancer. International Journal of Molecular Sciences, 22( 15), 1-14. doi:10.3390/ijms22157992
NLM
Inez DC de S, Fuziwara CS, Saito KC, Kimura ET. Targeting the highly expressed microRNA miR-146b with CRISPR/Cas9n gene editing system in thyroid cancer [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 15): 1-14.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/ijms22157992
Vancouver
Inez DC de S, Fuziwara CS, Saito KC, Kimura ET. Targeting the highly expressed microRNA miR-146b with CRISPR/Cas9n gene editing system in thyroid cancer [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 15): 1-14.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/ijms22157992
Artigo de periodico
The role of somatic mutations on the immune response of the tumor microenvironment in prostate cancer (2021)
Melo, Camila Morais ; Vidotto, Thiago ; Souza, Luiz Paulo Chaves; Lautert-Dutra, William ; Reis, Rodolfo Borges dos ; Squire, Jeremy Andrew
Source: International Journal of Molecular Sciences. Unidade: FMRP
Subjects: NEOPLASIAS PROSTÁTICAS, MUTAÇÃO, IMUNOTERAPIA, SISTEMA IMUNE, ONCOGENES, GENES SUPRESSORES DE TUMOR, GENÔMICA, MODELOS ANIMAIS DE DOENÇAS
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ABNT
MELO, Camila Morais et al. The role of somatic mutations on the immune response of the tumor microenvironment in prostate cancer. International Journal of Molecular Sciences, v. 22, n. 17, p. 1-19, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms22179550. Acesso em: 01 nov. 2024.
APA
Melo, C. M., Vidotto, T., Souza, L. P. C., Lautert-Dutra, W., Reis, R. B. dos, & Squire, J. A. (2021). The role of somatic mutations on the immune response of the tumor microenvironment in prostate cancer. International Journal of Molecular Sciences, 22( 17), 1-19. doi:10.3390/ijms22179550
NLM
Melo CM, Vidotto T, Souza LPC, Lautert-Dutra W, Reis RB dos, Squire JA. The role of somatic mutations on the immune response of the tumor microenvironment in prostate cancer [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 17): 1-19.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/ijms22179550
Vancouver
Melo CM, Vidotto T, Souza LPC, Lautert-Dutra W, Reis RB dos, Squire JA. The role of somatic mutations on the immune response of the tumor microenvironment in prostate cancer [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 17): 1-19.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/ijms22179550
Artigo de periodico
Mutational Profiling of Driver Tumor Suppressor and Oncogenic Genes in Brazilian Malignant Pleural Mesotheliomas (2020)
Campanella, Nathalia C; Silva, Eduardo Caetano; Dix, Gustavo; Vazquez, Fabiana de Lima; Paula, Flavia Escremim de; Berardinelli, Gustavo N; Balancin, Marcelo; Chammas, Roger ; Lopez, Rossana Mendoza Lopez; Capelozzi, Vera Luiza
Source: Pathobiology. Unidade: FM
Subjects: ASBESTO, MUTAÇÃO, ONCOGENES, GENES SUPRESSORES DE TUMOR
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CAMPANELLA, Nathalia C et al. Mutational Profiling of Driver Tumor Suppressor and Oncogenic Genes in Brazilian Malignant Pleural Mesotheliomas. Pathobiology, v. 87, n. 3, p. 208-215, 2020Tradução . . Disponível em: https://doi.org/10.1159/000507373. Acesso em: 01 nov. 2024.
APA
Campanella, N. C., Silva, E. C., Dix, G., Vazquez, F. de L., Paula, F. E. de, Berardinelli, G. N., et al. (2020). Mutational Profiling of Driver Tumor Suppressor and Oncogenic Genes in Brazilian Malignant Pleural Mesotheliomas. Pathobiology, 87( 3), 208-215. doi:10.1159/000507373
NLM
Campanella NC, Silva EC, Dix G, Vazquez F de L, Paula FE de, Berardinelli GN, Balancin M, Chammas R, Lopez RML, Capelozzi VL. Mutational Profiling of Driver Tumor Suppressor and Oncogenic Genes in Brazilian Malignant Pleural Mesotheliomas [Internet]. Pathobiology. 2020 ; 87( 3): 208-215.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000507373
Vancouver
Campanella NC, Silva EC, Dix G, Vazquez F de L, Paula FE de, Berardinelli GN, Balancin M, Chammas R, Lopez RML, Capelozzi VL. Mutational Profiling of Driver Tumor Suppressor and Oncogenic Genes in Brazilian Malignant Pleural Mesotheliomas [Internet]. Pathobiology. 2020 ; 87( 3): 208-215.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000507373
Artigo de periodico
Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation (2020)
Cavalcante, Isadora Pontes ; Vaczlavik, Anna; Drougat, Ludivine; Lotfi, Claudimara Ferini Pacicco ; Perlemoine, Karine; Ribes, Christopher; Rabin, Marthe Rizk ; Clauser, Eric ; Fragoso, Maria Candida Barisson Villares ; Bertherat, Jérôme ; Ragazzon, Bruno
Source: Endocrine - Related Cancer. Unidades: ICB, FM
Subjects: ANATOMIA, NEOPLASIAS DE TECIDO NERVOSO, MENINGIOMA, CÉLULAS CULTIVADAS DE TUMOR, GENES SUPRESSORES DE TUMOR, REGULAÇÃO NEOPLÁSICA DA EXPRESSÃO GÊNICA, TRANSCRIÇÃO GÊNICA, CICLO CELULAR, MUTAÇÃO GENÉTICA
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CAVALCANTE, Isadora Pontes et al. Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation. Endocrine - Related Cancer, v. 27, n. 4, p. 221-230, 2020Tradução . . Disponível em: https://doi.org/10.1530/ERC-19-0502. Acesso em: 01 nov. 2024.
APA
Cavalcante, I. P., Vaczlavik, A., Drougat, L., Lotfi, C. F. P., Perlemoine, K., Ribes, C., et al. (2020). Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation. Endocrine - Related Cancer, 27( 4), 221-230. doi:10.1530/ERC-19-0502
NLM
Cavalcante IP, Vaczlavik A, Drougat L, Lotfi CFP, Perlemoine K, Ribes C, Rabin MR, Clauser E, Fragoso MCBV, Bertherat J, Ragazzon B. Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation [Internet]. Endocrine - Related Cancer. 2020 ; 27( 4): 221-230.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1530/ERC-19-0502
Vancouver
Cavalcante IP, Vaczlavik A, Drougat L, Lotfi CFP, Perlemoine K, Ribes C, Rabin MR, Clauser E, Fragoso MCBV, Bertherat J, Ragazzon B. Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation [Internet]. Endocrine - Related Cancer. 2020 ; 27( 4): 221-230.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1530/ERC-19-0502
Artigo de periodico
ATR-FTIR spectroscopy and CDKN1C gene expression in the prediction of lymph nodes metastases in papillary thyroid carcinoma (2020)
Silva, Raissa Monteiro da; Pupin, Breno; Bhattacharjee, Tanmoy Tapobrata; Kulcsar, Marco Aurelio Vamondes; Uno, Miyuki; Chammas, Roger ; Canevari, Renata de Azevedo
Source: Spectrochimica acta part a-molecular and biomolecular spectroscopy. Unidade: FM
Subjects: ESPECTROSCOPIA INFRAVERMELHA, EXPRESSÃO GÊNICA, ADENOCARCINOMA PAPILAR, NEOPLASIAS DA TIREOIDE, PROTEÍNAS QUINASES, GENES SUPRESSORES DE TUMOR
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SILVA, Raissa Monteiro da et al. ATR-FTIR spectroscopy and CDKN1C gene expression in the prediction of lymph nodes metastases in papillary thyroid carcinoma. Spectrochimica acta part a-molecular and biomolecular spectroscopy, v. 228, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2019.117693. Acesso em: 01 nov. 2024.
APA
Silva, R. M. da, Pupin, B., Bhattacharjee, T. T., Kulcsar, M. A. V., Uno, M., Chammas, R., & Canevari, R. de A. (2020). ATR-FTIR spectroscopy and CDKN1C gene expression in the prediction of lymph nodes metastases in papillary thyroid carcinoma. Spectrochimica acta part a-molecular and biomolecular spectroscopy, 228. doi:10.1016/j.saa.2019.117693
NLM
Silva RM da, Pupin B, Bhattacharjee TT, Kulcsar MAV, Uno M, Chammas R, Canevari R de A. ATR-FTIR spectroscopy and CDKN1C gene expression in the prediction of lymph nodes metastases in papillary thyroid carcinoma [Internet]. Spectrochimica acta part a-molecular and biomolecular spectroscopy. 2020 ; 228[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.saa.2019.117693
Vancouver
Silva RM da, Pupin B, Bhattacharjee TT, Kulcsar MAV, Uno M, Chammas R, Canevari R de A. ATR-FTIR spectroscopy and CDKN1C gene expression in the prediction of lymph nodes metastases in papillary thyroid carcinoma [Internet]. Spectrochimica acta part a-molecular and biomolecular spectroscopy. 2020 ; 228[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.saa.2019.117693
Artigo de periodico
Inverse sex-based expression profiles of PTEN and Klotho in mice (2020)
Mello, Natalia Prudente de ; Andreotti, Diana Zukas; Orellana, Ana Maria Marques ; Scavone, Cristoforo ; Kawamoto, Elisa Mitiko
Source: Scientific Reports. Unidade: ICB
Subjects: FARMACOLOGIA, CAMUNDONGOS, GENES SUPRESSORES DE TUMOR, DIFERENÇAS SEXUAIS ANIMAL, APOPTOSE, PROTEÍNAS, REAÇÃO EM CADEIA POR POLIMERASE, WESTERN BLOTTING, IMUNOFLUORESCÊNCIA EM ANIMAL
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MELLO, Natalia Prudente de et al. Inverse sex-based expression profiles of PTEN and Klotho in mice. Scientific Reports, v. 10, p. 9 , 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-77217-5. Acesso em: 01 nov. 2024.
APA
Mello, N. P. de, Andreotti, D. Z., Orellana, A. M. M., Scavone, C., & Kawamoto, E. M. (2020). Inverse sex-based expression profiles of PTEN and Klotho in mice. Scientific Reports, 10, 9 . doi:10.1038/s41598-020-77217-5
NLM
Mello NP de, Andreotti DZ, Orellana AMM, Scavone C, Kawamoto EM. Inverse sex-based expression profiles of PTEN and Klotho in mice [Internet]. Scientific Reports. 2020 ; 10 9 .[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-020-77217-5
Vancouver
Mello NP de, Andreotti DZ, Orellana AMM, Scavone C, Kawamoto EM. Inverse sex-based expression profiles of PTEN and Klotho in mice [Internet]. Scientific Reports. 2020 ; 10 9 .[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-020-77217-5
Artigo de periodico
The highly expressed FAM83F Protein in papillary thyroid cancer exerts a pro-oncogenic role in thyroid follicular cells (2019)
Fuziwara, Cesar Seigi; Saito, Kelly Cristina; Leoni, Suzana Garcia; Waitzberg, Angela Flavia Logullo; Kimura, Edna Teruko
Source: Frontiers in Endocrinology. Unidade: ICB
Subjects: CÉLULAS-TRONCO, NEOPLASIAS DA TIREOIDE, DIFERENCIAÇÃO CELULAR, CÉLULAS CULTIVADAS DE TUMOR, GENES SUPRESSORES DE TUMOR, GLÂNDULA TIREOIDE, EXPRESSÃO GÊNICA, PROTEÍNAS PROTO-ONCOGÊNICAS
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FUZIWARA, Cesar Seigi et al. The highly expressed FAM83F Protein in papillary thyroid cancer exerts a pro-oncogenic role in thyroid follicular cells. Frontiers in Endocrinology, v. 10, p. 1-13, 2019Tradução . . Disponível em: https://doi.org/10.3389/fendo.2019.00134. Acesso em: 01 nov. 2024.
APA
Fuziwara, C. S., Saito, K. C., Leoni, S. G., Waitzberg, A. F. L., & Kimura, E. T. (2019). The highly expressed FAM83F Protein in papillary thyroid cancer exerts a pro-oncogenic role in thyroid follicular cells. Frontiers in Endocrinology, 10, 1-13. doi:10.3389/fendo.2019.00134
NLM
Fuziwara CS, Saito KC, Leoni SG, Waitzberg AFL, Kimura ET. The highly expressed FAM83F Protein in papillary thyroid cancer exerts a pro-oncogenic role in thyroid follicular cells [Internet]. Frontiers in Endocrinology. 2019 ; 10 1-13.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3389/fendo.2019.00134
Vancouver
Fuziwara CS, Saito KC, Leoni SG, Waitzberg AFL, Kimura ET. The highly expressed FAM83F Protein in papillary thyroid cancer exerts a pro-oncogenic role in thyroid follicular cells [Internet]. Frontiers in Endocrinology. 2019 ; 10 1-13.[citado 2024 nov. 01 ] Available from: https://doi.org/10.3389/fendo.2019.00134
Artigo de periodico
Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation (2019)
Ferreira, Amanda Meneses; Brondani, Vania Balderrama; Helena, Vanessa Petry; Charchar, Helaine Laiz Silva; Zerbini, Maria Claudia Nogueira ; Leite, Luiz Antonio Senna; Hoff, Ana Oliveira; Xavier, Ana Claudia Latronico ; Mendonça, Berenice Bilharinho de ; Diz, Maria Del Pilar Estevez
Source: Journal of steroid biochemistry and molecular biology. Unidade: FM
Subjects: NEOPLASIAS EPITELIAIS E GLANDULARES, GENES SUPRESSORES DE TUMOR, MUTAÇÃO GENÉTICA, HERANÇA GENÉTICA
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FERREIRA, Amanda Meneses et al. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation. Journal of steroid biochemistry and molecular biology, v. 190, p. 250-255, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2019.04.011. Acesso em: 01 nov. 2024.
APA
Ferreira, A. M., Brondani, V. B., Helena, V. P., Charchar, H. L. S., Zerbini, M. C. N., Leite, L. A. S., et al. (2019). Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation. Journal of steroid biochemistry and molecular biology, 190, 250-255. doi:10.1016/j.jsbmb.2019.04.011
NLM
Ferreira AM, Brondani VB, Helena VP, Charchar HLS, Zerbini MCN, Leite LAS, Hoff AO, Xavier ACL, Mendonça BB de, Diz MDPE. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation [Internet]. Journal of steroid biochemistry and molecular biology. 2019 ; 190 250-255.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jsbmb.2019.04.011
Vancouver
Ferreira AM, Brondani VB, Helena VP, Charchar HLS, Zerbini MCN, Leite LAS, Hoff AO, Xavier ACL, Mendonça BB de, Diz MDPE. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation [Internet]. Journal of steroid biochemistry and molecular biology. 2019 ; 190 250-255.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jsbmb.2019.04.011
Artigo de periodico
A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant (2019)
Gomes, Nathalia L.; Mendonça, Berenice Bilharinho de
Source: Clinical genetics. Unidade: FM
Subjects: ANORMALIDADES UROGENITAIS, GENES SUPRESSORES DE TUMOR, NEOPLASIAS RENAIS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Nathalia L. e MENDONÇA, Berenice Bilharinho de. A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant. Clinical genetics, v. 95, n. 1, p. 172-176, 2019Tradução . . Disponível em: https://doi.org/10.1111/cge.13459. Acesso em: 01 nov. 2024.
APA
Gomes, N. L., & Mendonça, B. B. de. (2019). A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant. Clinical genetics, 95( 1), 172-176. doi:10.1111/cge.13459
NLM
Gomes NL, Mendonça BB de. A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant [Internet]. Clinical genetics. 2019 ; 95( 1): 172-176.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1111/cge.13459
Vancouver
Gomes NL, Mendonça BB de. A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant [Internet]. Clinical genetics. 2019 ; 95( 1): 172-176.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1111/cge.13459
Artigo de periodico-carta/editorial
Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis [Carta] (2019)
Miyashiro, Denis; Torezan, Luis Antonio; Grinblat, Beni Moreinas; Festa Neto, Cyro
Source: Anais brasileiros de dermatologia. Unidade: FM
Subjects: SÍNDROME DO NEVO BASOCELULAR, ÚTERO, ANORMALIDADES CONGÊNITAS, GENES SUPRESSORES DE TUMOR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MIYASHIRO, Denis et al. Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis [Carta]. Anais brasileiros de dermatologia. Rio De Janeiro Rj: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1590/abd1806-4841.20197449. Acesso em: 01 nov. 2024. , 2019
APA
Miyashiro, D., Torezan, L. A., Grinblat, B. M., & Festa Neto, C. (2019). Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis [Carta]. Anais brasileiros de dermatologia. Rio De Janeiro Rj: Faculdade de Medicina, Universidade de São Paulo. doi:10.1590/abd1806-4841.20197449
NLM
Miyashiro D, Torezan LA, Grinblat BM, Festa Neto C. Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis [Carta] [Internet]. Anais brasileiros de dermatologia. 2019 ; 94( 4): 487-489.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/abd1806-4841.20197449
Vancouver
Miyashiro D, Torezan LA, Grinblat BM, Festa Neto C. Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis [Carta] [Internet]. Anais brasileiros de dermatologia. 2019 ; 94( 4): 487-489.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/abd1806-4841.20197449
Artigo de periodico-carta/editorial
Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor [Carta] (2019)
Aguiar, Talita Ferreira; Barbosa-teixeira, Anne C; Costa, Silvia Souza; Ezquina, Suzana; Gimenez, Thamiris Magalhaes; Novak, Estela; Cristofani, Lilian Maria; Rosenberg, Carla ; Odone Filho, Vicente; Krepischi, Ana Cristina Victorino
Source: Pediatric blood & cancer. Unidade: FM
Subjects: PÓLIPOS ADENOMATOSOS, NEOPLASIAS CEREBRAIS, GENES SUPRESSORES DE TUMOR, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUIAR, Talita Ferreira et al. Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor [Carta]. Pediatric blood & cancer. Hoboken: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/pbc.27566. Acesso em: 01 nov. 2024. , 2019
APA
Aguiar, T. F., Barbosa-teixeira, A. C., Costa, S. S., Ezquina, S., Gimenez, T. M., Novak, E., et al. (2019). Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor [Carta]. Pediatric blood & cancer. Hoboken: Faculdade de Medicina, Universidade de São Paulo. doi:10.1002/pbc.27566
NLM
Aguiar TF, Barbosa-teixeira AC, Costa SS, Ezquina S, Gimenez TM, Novak E, Cristofani LM, Rosenberg C, Odone Filho V, Krepischi ACV. Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor [Carta] [Internet]. Pediatric blood & cancer. 2019 ; 66( 4):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/pbc.27566
Vancouver
Aguiar TF, Barbosa-teixeira AC, Costa SS, Ezquina S, Gimenez TM, Novak E, Cristofani LM, Rosenberg C, Odone Filho V, Krepischi ACV. Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor [Carta] [Internet]. Pediatric blood & cancer. 2019 ; 66( 4):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/pbc.27566
Artigo de periodico
Comprehensive molecular characterization of the hippo signaling pathway in cancer (2018)
Noushmer, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankuty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell Reports. Unidade: FMRP
Subjects: NEOPLASIAS, PROGNÓSTICO, GENES SUPRESSORES DE TUMOR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOUSHMER, Houtan et al. Comprehensive molecular characterization of the hippo signaling pathway in cancer. Cell Reports, v. 25, n. 5, p. 1304-1317, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.celrep.2018.10.001. Acesso em: 01 nov. 2024.
APA
Noushmer, H., Carlotti Júnior, C. G., Santos, J. S. dos, Kemp, R., Sankarankuty, A. K., & Tirapelli, D. P. da C. (2018). Comprehensive molecular characterization of the hippo signaling pathway in cancer. Cell Reports, 25( 5), 1304-1317. doi:10.1016/j.celrep.2018.10.001
NLM
Noushmer H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankuty AK, Tirapelli DP da C. Comprehensive molecular characterization of the hippo signaling pathway in cancer [Internet]. Cell Reports. 2018 ; 25( 5): 1304-1317.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.celrep.2018.10.001
Vancouver
Noushmer H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankuty AK, Tirapelli DP da C. Comprehensive molecular characterization of the hippo signaling pathway in cancer [Internet]. Cell Reports. 2018 ; 25( 5): 1304-1317.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.celrep.2018.10.001
Artigo de periodico
Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections (2018)
Yoshimoto, Maisa; Ludkovski, Olga; Good, Jennifer; Pereira, Ciro; Gooding, Robert J.; McGowan-Jordan, Jean; Boag, Alexander; Evans, Andrew; Tsao, Ming-Sound; Nuin, Paulo; Squire, Jeremy Andrew
Source: Laboratory Investigation. Unidade: FMRP
Subjects: DELEÇÃO DE GENES, HIBRIDIZAÇÃO, GENES SUPRESSORES DE TUMOR, NEOPLASIAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YOSHIMOTO, Maisa et al. Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections. Laboratory Investigation, v. 98, n. 4, p. 403-413, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41374-017-0007-2. Acesso em: 01 nov. 2024.
APA
Yoshimoto, M., Ludkovski, O., Good, J., Pereira, C., Gooding, R. J., McGowan-Jordan, J., et al. (2018). Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections. Laboratory Investigation, 98( 4), 403-413. doi:10.1038/s41374-017-0007-2
NLM
Yoshimoto M, Ludkovski O, Good J, Pereira C, Gooding RJ, McGowan-Jordan J, Boag A, Evans A, Tsao M-S, Nuin P, Squire JA. Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections [Internet]. Laboratory Investigation. 2018 ; 98( 4): 403-413.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41374-017-0007-2
Vancouver
Yoshimoto M, Ludkovski O, Good J, Pereira C, Gooding RJ, McGowan-Jordan J, Boag A, Evans A, Tsao M-S, Nuin P, Squire JA. Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections [Internet]. Laboratory Investigation. 2018 ; 98( 4): 403-413.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41374-017-0007-2
Artigo de periodico
Intermittent fasting uncovers and rescues cognitive phenotypes in PTEN neuronal haploinsufficient mice (2018)
Costa, João Victor Cabral ; Andreotti\202C\202A, Diana Zukas; Mello, Natalia Prudente de ; Scavone, Cristoforo ; Camandola, S. ; Kawamoto, Elisa Mitiko
Source: Scientific Reports. Unidades: ICB, IQ
Subjects: FARMACOLOGIA, HAPLOTIPOS, GENÓTIPOS, GENES SUPRESSORES DE TUMOR, PLASTICIDADE NEURONAL, MUTAÇÃO GENÉTICA, PROCESSOS COGNITIVOS, COMPORTAMENTO ANIMAL, CÉLULAS CULTIVADAS DE TUMOR, MEMÓRIA ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, João Victor Cabral et al. Intermittent fasting uncovers and rescues cognitive phenotypes in PTEN neuronal haploinsufficient mice. Scientific Reports, v. 8, p. 1-13, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-26814-6. Acesso em: 01 nov. 2024.
APA
Costa, J. V. C., Andreotti\202C\202A, D. Z., Mello, N. P. de, Scavone, C., Camandola, S., & Kawamoto, E. M. (2018). Intermittent fasting uncovers and rescues cognitive phenotypes in PTEN neuronal haploinsufficient mice. Scientific Reports, 8, 1-13. doi:10.1038/s41598-018-26814-6
NLM
Costa JVC, Andreotti\202C\202A DZ, Mello NP de, Scavone C, Camandola S, Kawamoto EM. Intermittent fasting uncovers and rescues cognitive phenotypes in PTEN neuronal haploinsufficient mice [Internet]. Scientific Reports. 2018 ; 8 1-13.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-018-26814-6
Vancouver
Costa JVC, Andreotti\202C\202A DZ, Mello NP de, Scavone C, Camandola S, Kawamoto EM. Intermittent fasting uncovers and rescues cognitive phenotypes in PTEN neuronal haploinsufficient mice [Internet]. Scientific Reports. 2018 ; 8 1-13.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-018-26814-6
Artigo de periodico
Cost effectiveness of the cancer prevention program for carriers of the BRCA1/2 mutation (2018)
Ramos, Marcelo Cristiano de Azevedo; Folgueira, Maria Aparecida Azevedo Koike; Maistro, Simone; Campolina, Alessandro Goncalves; Soarez, Patricia Coelho de; Bock, Geertruida Hendrika de; Novaes, Hillegonda Maria Dutilh; Diz, Maria Del Pilar Estevez
Source: Revista de saude publica. Unidade: FM
Subjects: SOBREVIDA, NEOPLASIAS OVARIANAS, MUTAÇÃO GENÉTICA, GENES SUPRESSORES DE TUMOR, CUSTOS DOS CUIDADOS DE SAÚDE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Marcelo Cristiano de Azevedo et al. Cost effectiveness of the cancer prevention program for carriers of the BRCA1/2 mutation. Revista de saude publica, v. 52, 2018Tradução . . Disponível em: https://doi.org/10.11606/S1518-8787.2018052000643. Acesso em: 01 nov. 2024.
APA
Ramos, M. C. de A., Folgueira, M. A. A. K., Maistro, S., Campolina, A. G., Soarez, P. C. de, Bock, G. H. de, et al. (2018). Cost effectiveness of the cancer prevention program for carriers of the BRCA1/2 mutation. Revista de saude publica, 52. doi:10.11606/S1518-8787.2018052000643
NLM
Ramos MC de A, Folgueira MAAK, Maistro S, Campolina AG, Soarez PC de, Bock GH de, Novaes HMD, Diz MDPE. Cost effectiveness of the cancer prevention program for carriers of the BRCA1/2 mutation [Internet]. Revista de saude publica. 2018 ; 52[citado 2024 nov. 01 ] Available from: https://doi.org/10.11606/S1518-8787.2018052000643
Vancouver
Ramos MC de A, Folgueira MAAK, Maistro S, Campolina AG, Soarez PC de, Bock GH de, Novaes HMD, Diz MDPE. Cost effectiveness of the cancer prevention program for carriers of the BRCA1/2 mutation [Internet]. Revista de saude publica. 2018 ; 52[citado 2024 nov. 01 ] Available from: https://doi.org/10.11606/S1518-8787.2018052000643

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